QUINTREX 0516 PROG. PULSE GENERATOR SYS— 510(k) K802224

Unknown

Medcor, Inc.

FDA 510(k) clearance K802224 for QUINTREX 0516 PROG. PULSE GENERATOR SYS, Unknown on 1980-09-12. Applicant: Medcor, Inc..

Clearance details

Applicant: Medcor, Inc.
Advisory panel: Unknown
Date received: 1980-09-12
Decision date: 1980-09-12
Decision: Unknown
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.